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Status |
Public on May 26, 2024 |
Title |
Pseudomonas aeruginosa Activates Quorum Sensing, Antioxidant Enzymes and Type VI Secretion in Response to Oxidative Stress to Initiate Biofilm Formation and Wound Chronicity |
Organism |
Pseudomonas aeruginosa |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Pseudomonas aeruginosa (PA) is an opportunistic pathogen frequently isolated from cutaneous chronic wounds. How PA, in the presence of oxidative stress (OS), colonizes chronic wounds and forms a biofilm is still unknown. The purpose of this study is to investigate the changes in gene expression seen when PA is challenged with the high levels of OS present in chronic wounds. We used a biofilm-forming PA strain isolated from the chronic wounds of our murine model (RPA) and performed a qPCR to obtain gene expression patterns as RPA developed a biofilm in vitro in the presence of high levels of OS, and then compared the findings in vivo, in our mouse model of chronic wounds. We found that the planktonic bacteria under OS conditions overex-pressed quorum sensing genes that are important for the bacteria to communicate with each other, antioxidant stress genes important to reduce OS in the microenvironment for survival, biofilm formation genes and virulence genes. Additionally, we performed RNAseq in vivo and identified the activation of novel genes/pathways of the Type VI Secretion System (T6SS) involved in RPA pathogenicity. In conclusion, RPA appears to survive the high OS microenvironment in chronic wounds and colonizes these wounds by turning on virulence, biofilm-forming and survival genes. These findings reveal pathways that may be promising targets for new therapies aimed at dis-rupting PA-containing biofilms immediately after debridement to facilitate the treatment of chronic human wounds.
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Overall design |
RNAseq of Psuedomonas aeruginosa collected from nonchronic (control) and chronic wounds to understand the transcriptomic regulation of PA during infection in response to high levels of oxidative stress.
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Contributor(s) |
Martins-Green M, Kim J |
Citation(s) |
38929094 |
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Submission date |
May 20, 2024 |
Last update date |
Jul 31, 2024 |
Contact name |
Manuela Martins-Green |
Organization name |
University of California, Riverside
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Street address |
900 University Ave
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City |
Riverside |
State/province |
CA |
ZIP/Postal code |
92521 |
Country |
USA |
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Platforms (1) |
GPL33271 |
NextSeq 2000 (Pseudomonas aeruginosa) |
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Samples (18)
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Relations |
BioProject |
PRJNA1113559 |